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Applied and Environmental Microbiology, March 2000, p. 1237-1242, Vol. 66, No. 3
Unigen and Department of Botany, Norwegian
University of Science and Technology, 7491 Trondheim,
Norway1; Research Institute for Plant
Protection, IPO-DLO, 6700 GW Wageningen, The
Netherlands2; and Institute for
Plant Virology, Microbiology and Biosafety, Federal Biological Research
Centre for Agriculture and Forestry, (BBA), 38104 Braunschweig,
Germany3
Received 1 November 1999/Accepted 27 December 1999
Here we show that horizontal transfer of DNA, extracted from
transgenic sugar beets, to bacteria, based on homologous recombination, can occur in soil. Restoration of a 317-bp-deleted nptII
gene in Acinetobacter sp. strain BD413(pFG4) cells
incubated in sterile soil microcosms was detected after addition of
nutrients and transgenic plant DNA encoding a functional
nptII gene conferring bacterial kanamycin resistance.
Selective effects of the addition of kanamycin on the population
dynamics of Acinetobacter sp. cells in soil were found, and
high concentrations of kanamycin reduced the CFU of
Acinetobacter sp. cells from 109 CFU/g of soil
to below detection. In contrast to a chromosomal nptII-encoded kanamycin resistance, the pFG4-generated
resistance was found to be unstable over a 31-day incubation period in vitro.
0099-2240/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Transformation of Acinetobacter sp.
Strain BD413(pFG4
nptII) with Transgenic Plant DNA in Soil
Microcosms and Effects of Kanamycin on Selection of
Transformants
*
Corresponding author. Present address: D. Hartl
Laboratory, Department of Organismic and Evolutionary Biology, Harvard
University, 16 Divinity Ave., Cambridge, MA 02138. Phone: (617)
496-5540. Fax: (617) 496-5854. E-mail:
knielsen{at}oeb.harvard.edu.
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